Diverse Biosynthetic Pathways and Protective Functions against Environmental Stress of Antioxidants in Microalgae

Eukaryotic microalgae have been classified into several biological divisions and have evolutionarily acquired diverse morphologies, metabolisms, and life cycles. They are naturally exposed to environmental stresses that cause oxidative damage due to reactive oxygen species accumulation. To cope with environmental stresses, microalgae contain various antioxidants, including carotenoids, ascorbate (AsA), and glutathione (GSH). Carotenoids are hydrophobic pigments required for light harvesting, photoprotection, and phototaxis. AsA constitutes the AsA-GSH cycle together with GSH and is responsible for photooxidative stress defense. GSH contributes not only to ROS scavenging, but also to heavy metal detoxification and thiol-based redox regulation. The evolutionary diversity of microalgae influences the composition and biosynthetic pathways of these antioxidants. For example, α-carotene and its derivatives are specific to Chlorophyta, whereas diadinoxanthin and fucoxanthin are found in Heterokontophyta, Haptophyta, and Dinophyta. It has been suggested that AsA is biosynthesized via the plant pathway in Chlorophyta and Rhodophyta and via the Euglena pathway in Euglenophyta, Heterokontophyta, and Haptophyta. The GSH biosynthetic pathway is conserved in all biological kingdoms; however, Euglenophyta are able to synthesize an additional thiol antioxidant, trypanothione, using GSH as the substrate. In the present study, we reviewed and discussed the diversity of microalgal antioxidants, including recent findings.


Introduction
Eukaryotic microalgae (excluding prokaryotic microalgae in this review) are classified into various phylogenetic divisions, including Chlorophyta (e.g., Chlamydomonas reinhardtii and Chlorella vulgaris), Rhodophyta (e.g., Cyanidioschyzon merolae), Heterokontophyta (e.g., the diatom Phaeodactylum tricornutum), Haptophyta (e.g., Emiliania huxleyi), Dinophyta (e.g., Symbiodinium minutum), and Euglenophyta (e.g., Euglena gracilis) [1]; their evolution, morphology, habitat, and metabolism are extremely diverse. Although the genomes of C. reinhardtii and C. merolae were sequenced prior to the genomes of other algal species [2,3], research using limited algal species is not sufficient to understand the biology of diverse microalgae. To gain this understanding, a wide range of algal species needs to be studied. Notably, as microalgae have photosynthetic ability, fast and autotrophic growth, and various material productivity, they have recently attracted attention because their biomass can be used to produce food, fuel, and other valuable materials, and outdoor culture equipment has been developed [4][5][6]. Under outdoor culture conditions, microalgae cannot avoid fluctuating environmental stresses, such as high light, low and high temperatures, and UV irradiation. Exposure to these environmental stresses increases the accumulation of

Carotenoid Biosynthesis
In eukaryotic microalgae, the biosynthetic pathway from phytoene to lycopene is conserved, whereas the downstream pathway from lycopene to each end carotenoid compound is diverse, as reviewed below ( Figure 1).

Carotenoid Biosynthesis
In eukaryotic microalgae, the biosynthetic pathway from phytoene to lycopene is conserved, whereas the downstream pathway from lycopene to each end carotenoid compound is diverse, as reviewed below ( Figure 1).

α-Carotene and Derivatives Synthesis
Lycopene is cyclized at both ends by lycopene cyclase (LCY). Distinct LCYb and LCYe enzymes generally form a β-ring at one end and an ε-ring at the other end of α-carotene, respectively [27]. A recent study reported that LCYb and LCYe from Dunaliella bardawil exhibit both βand ε-cyclase activities [28]. Ostreococcus lucimarinus and its relatives have a unique gene encoding LCYb, LCYe, and a C-terminal light-harvesting complex (LHC, see Section 2.3.1) domain fusion protein in a single polypeptide [29]. α-Carotene is then hydroxylated to lutein by nonheme/di-iron carotene hydroxylase (BCH) and heme-containing cytochrome P450-type carotene hydroxylase (CYP97). BCH and CYP97A have hydroxylation activity towards the β-ring of α-carotene, and CYP97C have a hydroxylation activity towards the ε-ring of α-carotene [30,31]. The LCYb and CYP97 family enzymes are widely distributed in microalgae, whereas LCYe and CYP97C are involved in ε-ring formation and hydroxylation in Chlorophyta [32]. Therefore, the α-carotene, lutein, and downstream carotenoid compound synthetic pathways are specific to Chlorophyta. Loroxanthin, siphonaxanthin, prasinoxanthin, and monadoxanthin are considered to be synthesized from lutein, but the genes involved in their synthesis have not yet been identified.

β-Carotene and Derivatives Synthesis
β-Carotene is produced by β-cyclization of lycopene at both ends. LCYb generally catalyzes this reaction [33], and LCYb genes are found in all microalgae. The β-rings of β-carotene are hydroxylated by BCH, CYP97, and CrtR (which is a third-type β-carotene hydroxylase homologous to BCH) to produce zeaxanthin. This step is highly diversified in carotenoid biosynthesis. Chlorophyta species have two types of β-carotene hydroxylases, BCH and CYP97A [31,34]. The microphytic red alga C. merolae possesses the crtR gene and lacks the BCH and CYP97 genes [15]. In Heterokontophyta, Haptophyta, Dinophyta, and Euglenophyta, CYP97s (clans E, F, G, and H) are the sole β-carotene hydroxylases [32,35,36]. Lycopene β-cyclases and β-carotene hydroxylases have been demonstrated to be physiologically important for various environmental stress responses in microalgae. The halotolerant green alga D. salina upregulates the LCYb gene to accumulate β-carotene when exposed to saline, high light, and nitrogen depletion stresses [37]. In P. tricornutum, CYP97 gene expression is induced in response to high light in order to accumulate β-carotene derivatives, fucoxanthin and diatoxanthin [35]. Our reverse genetic analysis revealed that E. gracilis CYP97H1 is essential for carotenoid synthesis and chloroplast homeostasis [36].
Astaxanthin is produced by hydroxylation and ketolation of β-carotene at both β-rings. The ketolation reactions are catalyzed by β-carotene ketolase (CrtW/BKT) [10,11]. The crtW genes have been identified in Chlorophyta H. pluvialis and C. zofingiensis [44,45]. It has been reported that C. zofingiensis accumulates astaxanthin under high light, nitrogen deprivation, and high salinity conditions by upregulating BCH and crtW gene expression [46][47][48]. Carotenoids bind to light-harvesting complexes (LHCs) with chlorophylls. Carotenoids in LHC promote photosynthesis by absorbing blue-green light and transferring energy to nearby chlorophylls [49]. The efficiency of this energy transfer varies depending on the carotenoid and chlorophyll compositions in the LHC. In addition to LHC, fucoxanthinchlorophyll a/c binding proteins (FCP) in diatoms [50,51] and the peridinin-chlorophyll a protein complex (PCP) in dinoflagellates [52,53] also act as light-harvesting complexes binding specific carotenoids.

Photoprotection
When photoexcited, chlorophyll transitions to the triplet state, after which it generates singlet oxygen by transferring energy from triplet chlorophyll to oxygen molecules. Singlet oxygen may damage the D1 subunit of photosystem II (PSII) and inhibit the repair of this subunit, leading to photoinhibition [54,55]. Carotenoids suppress singlet oxygen generation by receiving excess energy from triplet chlorophyll and dissipating this energy as heat. Carotenoids also directly receive energy from singlet oxygen and scavenge it [56].
In fact, C. reinhardtii mutant lacking carotenoid (the FN68 strain) is sensitive to light and unable to accumulate LHCs associated with both photosystems [57], demonstrating that quenching capacities of carotenoids against triplet chlorophyll and singlet oxygen contribute to photoprotection.

Xanthophyll Cycles
Xanthophyll cycles control non-photochemical quenching (NPQ), which dissipates excessive light energy in the form of heat under high light conditions. There are two types of xanthophyll cycles: the violaxanthin cycle found in Chlorophyta and the diadinoxanthin cycle found in Heterokontophyta, Haptophyta, Dinophyta, and Euglenophyta. In the violaxanthin cycle, violaxanthin bound to the LHC of PSII is converted to zeaxanthin via antheraxanthin by violaxanthin de-epoxidase (VDE) under high light conditions to reduce the light harvesting efficiency ( Figure 1). Under low light or dark conditions, zeaxanthin is converted back to violaxanthin via antheraxanthin by zeaxanthin epoxidase (ZEP) (Figure 1). Similarly, in the diadinoxanthin cycle, diadinoxanthin is converted to diatoxanthin by diadinoxanthin de-epoxidase (DDE) under high light conditions, and the reverse reaction is performed by diatoxanthin epoxidase (DEP) under low light or dark conditions. In Chlorophyta, C. reinhardtii VDE converts violaxanthin to zeaxanthin under high light conditions; however, it is not required for high light acclimation [39]. In contrast, C. vulgaris VDE-mediated zeaxanthin accumulation is crucial for the induction of NPQ under high light, suggesting diverse evolution of the violaxanthin cycle among Chlorophyta [58]. In diatoms, a silencing study suggested that P. tricornutum DDE, a VDE homolog, catalyzes diadinoxanthin de-epoxidation and induces NPQ under high light [59]. Moreover, it was reported that the culturing of E. gracilis at low temperatures results in photosensitivity and an increase in the ratio of diatoxanthin/diadinoxanthin, suggesting a functional diadinoxanthin cycle in Euglenophyta [60].

Stabilization of Lipid Membranes
In microalgae, physical properties of lipid membranes are associated with cellular processes and environmental stress tolerance. Notably, the physical properties of thylakoid membranes affect the photosynthetic activity. Hydrophobic carotenoids are incorporated into lipid membranes, and xanthophylls containing polar groups at both ends are oriented across the lipid membranes. These carotenoids modify membrane fluidity and enhance its stability [61,62]. Physiological evidence of carotenoid-mediated membrane stability has been documented in violaxanthin de-epoxidation in plants [63]. A recent study reported that diadinoxanthin de-epoxidation in the thylakoid membrane of P. tricornutum causes membrane rearrangement and confers stabilization and rigidification to membranes [64]. Carotenoids are also major components of eyespot globules found in flagellated microalgae and are essential for phototactic responses. Phototaxis is a responsive movement in which the swimming direction changes to optimize photosynthetic activity depending on the light intensity [65,66]. In C. reinhardtii, an eyespot is formed in the chloroplasts, and two carotenoid-rich layers reflect light from outside the cell and amplify the light signal received by the photoreceptor, or they shade light from inside the cell to accurately recognize the light direction [67]. The eyespot of E. gracilis is positioned in the cytosol near the base of the major flagellum, its development is independent of chloroplast development, and it has been demonstrated that its presence is required for initiating phototaxis [21,68]. These findings suggest that eyespot position and physiological function differ between Chlorophyta and Euglenophyta.

Ascorbate
The hydrophilic antioxidant ascorbate (AsA) accumulates at high (millimolar) concentrations in cells and plays a crucial role in photooxidative stress defense in all microalgae.

Ascorbate Biosynthesis
Photosynthetic organisms and most animals, except for humans and some others, can synthesize AsA. In photosynthetic organisms, AsA biosynthetic pathways are classified into the plant pathway (also called the D-mannose/L-galactose pathway) and the Euglena pathway (also called the D-galacturonate pathway).
All of these plant pathway genes have been identified in A. thaliana and have been reported to be conserved in Chlorophyta C. reinhardtii, V. carteri, Chlorella sp. NC64A, and Coccomyxa sp. C169 [74]. The enzymatic property of C. reinhardtii VTC2, a key enzyme of the plant pathway, was found to be similar to those of A. thaliana VTC2, and its knockdown resulted in a 90% decrease in AsA content. Moreover, in C. reinhardtii, the transition from dark to light, high light irradiation, and H 2 O 2 treatment caused VTC2 gene upregulation and AsA accumulation [74,75]. These findings suggested that AsA synthesis via the plant pathway protects C. reinhardtii cells from photooxidative stress.
In contrast to land plants and Chlorophyta, Rhodophyta lack the VTC2 homologous gene. However, supplementation experiments of plant pathway intermediates and positional isotopic labeling approach suggested that Rhodophyta synthesized AsA via a plant-like pathway. Therefore, Rhodophyta may use a modified plant pathway by the catalysis of an unidentified enzyme that converts GDP-L-galactose to L-galactose instead of VTC2 [70].
plant pathway protects C. reinhardtii cells from photooxidative stress.
In contrast to land plants and Chlorophyta, Rhodophyta lack the VTC2 homologous gene. However, supplementation experiments of plant pathway intermediates and positional isotopic labeling approach suggested that Rhodophyta synthesized AsA via a plantlike pathway. Therefore, Rhodophyta may use a modified plant pathway by the catalysis of an unidentified enzyme that converts GDP-L-galactose to L-galactose instead of VTC2 [70].

Euglena Pathway
The Euglena pathway was proposed after the detection of D-galacturonate and Lgalactono-1,4-lactone as AsA biosynthesis intermediates in E. gracilis (Figure 2) [76]. This pathway was then supported by genetic and biochemical characterizations of Dgalacturonic acid reductase (GalUAR) and aldonolactonase (ALase) in E. gracilis [77,78]. GalUAR reduces D-galacturonate to L-galactonate, which is then converted to L-galactono-1,4-lactone by ALase. The final step that converts L-galactono-1,4-lactone to AsA by GLDH is common in both plant and Euglena pathways. The fact that growth inhibition of ALase-knockdown E. gracilis can be counteracted by supplementation with L-galactono-1,4-lactone indicated that in E. gracilis, the Euglena pathway is predominantly utilized for AsA biosynthesis [78]. The Euglena pathway-specific ALase gene is homologous to that in the diatoms P. tricornutum and Thalassiosira pseudonana, but not to that in A. thaliana, C. reinhardtii, and V. carteri, suggesting the utilization of this pathway in diatoms [78]. Genome sequencing and phylogenetic analyses predicted that Heterokontophyta other than diatoms, Haptophyta, and Cryptophyta also use the Euglena pathway [70,79,80].
In E. gracilis, light irradiation induces ALase activity and AsA accumulation [78]. The photoinduction of AsA in this algal species is specific to blue light, but not to red and green light [81]. In the diatom Skeletonema marinoi, strong blue light irradiation induces AsA synthesis along with the synthesis of photosynthetic pigments [82]. Therefore, AsA biosynthesis is considered to be sensitive to the light environment in a wide range of microalgae, regardless of whether they drive either plant or Euglena pathways.

Ascorbate Peroxidase and the Ascorbate-regenerating System
AsA is an electron donor of the ROS-scavenging enzyme ascorbate peroxidase (APX) which catalyzes the reduction of H 2 O 2 to H 2 O and prevents oxidative stress damage in cells ( Figure 3) [83,84]. The rate constant of APX for scavenging H 2 O 2 (10 7 ) is much higher than that of AsA itself (up to 6); thus, APX activity allows rapid avoidance of H 2 O 2 toxicity [8]. APX also has a reduction activity towards organic hydroperoxides, but this activity is lower than that of H 2 O 2 [83,85], suggesting that APX is an enzyme specialized for H 2 O 2 scavenging. Figure 3) [83,84]. The rate constant of APX for scavenging H2O2 (10 7 ) is much highe than that of AsA itself (up to 6); thus, APX activity allows rapid avoidance of H2O2 toxicit [8]. APX also has a reduction activity towards organic hydroperoxides, but this activity i lower than that of H2O2 [83,85], suggesting that APX is an enzyme specialized for H2O scavenging.

cells (
During the APX reaction, APX simultaneously produces monodehydroascorbat (MDA), which is a univalent oxidant of AsA. MDA is then spontaneously disproportion ated to AsA and dehydroascorbate (DHA), a divalent oxidant of AsA. MDA and DHA ar reduced back to AsA by MDA reductase (MDAR) using NADPH as an electron donor and DHA reductase (DHAR) using glutathione (GSH) as an electron donor, respectively The resulting oxidized form of glutathione (GSSG) is reduced back to GSH by glutathion reductase (GR) using NADPH as an electron donor. This AsA-regenerating system i termed the AsA-GSH cycle and is essential for maintaining AsA redox homeostasis (Fig  ure 3) [84,86].  During the APX reaction, APX simultaneously produces monodehydroascorbate (MDA), which is a univalent oxidant of AsA. MDA is then spontaneously disproportionated to AsA and dehydroascorbate (DHA), a divalent oxidant of AsA. MDA and DHA are reduced back to AsA by MDA reductase (MDAR) using NADPH as an electron donor, and DHA reductase (DHAR) using glutathione (GSH) as an electron donor, respectively. The resulting oxidized form of glutathione (GSSG) is reduced back to GSH by glutathione reductase (GR) using NADPH as an electron donor. This AsA-regenerating system is termed the AsA-GSH cycle and is essential for maintaining AsA redox homeostasis ( Figure 3) [84,86].
The number and localization (including predictions) of some microalgae AsA-GSH cycle enzymes have been documented. C. reinhardtii contains three APX isoforms; APX1 and APX2 were predicted to be dual-targeted in chloroplasts and mitochondria, and APX4 in chloroplasts [87]. Single MDAR and DHAR enzymes are present in C. reinhardtii, and they are probably located in the cytosol [88,89]. C. reinhardtii GRs are composed of two isoforms [90]. E. gracilis contains APX, MDAR, DHAR, and GR enzymes as a single isoform, all of which are localized in the cytosol [91][92][93]. Therefore, AsA regeneration is functional only in the cytosol, at least in C. reinhardtii and E. gracilis. In other microalgal species, two APX isoforms in the cytosol and chloroplasts of C. merolae and four APX isoforms in the cytosol and peroxisomes of Galdieria sulphuraria have been reported [94]. In contrast to microalgae, A. thaliana contains more AsA-GSH cycle enzyme sets, which are composed of eight APX, five MDAR, three DHAR, and two GR isoforms and are widely distributed in the cytosol, chloroplasts, mitochondria, and peroxisomes [95]. Microalgae that live in water environments are less exposed to oxygen and light, which stimulates ROS generation than that in land plants. Thus, it can be presumed that in microalgae, the number and localization of AsA-GSH cycle enzymes were more limited than those in land plants during evolution.
A recent study reported that in C. reinhardtii, the expression of APX genes is induced under high light stress, and a knockdown of chloroplastic APX4 caused sensitivity to photooxidative stress [87]. Moreover, overexpression and knockdown of MDAR and DHAR genes in C. reinhardtii resulted in tolerance and sensitivity to high light stress, respectively [88,89]. In E. gracilis, APX-knockdown cells showed high H 2 O 2 accumulation [91]. These findings demonstrated that the microalgal AsA-GSH cycle plays a key role in photooxidative stress defense.

Reductant for Xanthophyll Cycles
Furthermore, AsA is used as a reductant of VDE and DDE reactions in xanthophyll cycles and is thus required for maintaining appropriate NPQ levels in photosynthetic organisms (see Section 2.3.3.) [96]. It has been reported that in C. vulgaris and P. tricornutum, VDE enzymes are active in the presence of AsA in vitro [58,97]. However, a recent study using C. reinhardtii demonstrated that AsA deficiency caused by vtc2 knockout does not limit violaxanthin de-epoxidation and NPQ induction [98]. Therefore, the role of AsA as a reductant in the xanthophyll cycle of microalgae remains controversial.

Glutathione
GSH is a low molecular weight thiol tripeptide found in all organisms. It is composed of Glu, Cys, and Gly, plays an important role as a hydrophilic antioxidant and thiol-based redox regulator, and is essential for the survival of microalgae. It is also used for the biosynthesis of phytochelatins and trypanothione (GSH derivatives).

Glutathione Biosynthesis
GSH is synthesized in two ATP-dependent steps catalyzed by γ-glutamylcysteine synthetase (GSH1, also abbreviated as γECS) and glutathione synthetase (GSH2, also abbreviated as GS). In the first step, GSH1 ligates Cys with Glu to produce γEC. In the second step, Gly is ligated to γ-EC by GSH2 to yield GSH [99] (Figure 4). Two GSH biosynthesis genes are conserved in all biological kingdoms. Genetic and physiological analyses using A. thaliana mutants have demonstrated that both GSH1 and GSH2 are essential for the development of plant roots and seedlings [100,101]. One study reported that glutathione synthesis in E. gracilis grown in the dark was photoinduced post-transcriptionally [102]. In Chlorophyta, glutathione synthesis is downregulated by cold and superoxide generator treatment in D. viridis [103] and by high light in C. reinhardtii [89]. These findings suggested that microalgae acclimate to environmental stresses by altering cellular glutathione levels. However, to our knowledge, the glutathione synthetic genes in microalgae have not yet been characterized, and thus, the physiological significance of glutathione synthesis is poorly understood.

Glutathione Peroxidase
Glutathione peroxidase (GPX) is an antioxidant enzyme that reduces H 2 O 2 , organic hydroperoxides and lipid peroxides, and detoxifies them using GSH or thioredoxin (Trx) as electron donors. During the GPX reaction, GSSG and oxidized Trx are reduced by GR and NADPH-dependent Trx reductase (NTR) ( Figure 5A). GPX is classified into two types: enzyme-containing selenocysteine (SeCys) at the catalytic site and enzyme without SeCys [104,105]. C. reinhardtii contains five genes encoding GPXs, including both SeCyscontaining (GPX1 and GPX2) and non-selenium GPXs (GPX3, GPX4, and GPX5). These GPX enzymes are predicted to be distributed in cellular compartments, including the cytosol, chloroplasts, and mitochondria [106,107]. To date, their functional characterization has been focused on C. reinhardtii GPX5, which uses Trx as an electron donor, and its gene expression is responsive to high light and singlet oxygen generators [108]. Knockout of GPX5 in C. reinhardtii causes ROS accumulation and thereby arrests growth, suggesting the crucial role of GPX5 as an antioxidant enzyme [109]. However, little is known about the physiological functions of GSH-dependent GPX in C. reinhardtii. Chlorella sp. NJ-18 contains two genes encoding non-selenium GPXs, which use Trx as an electron donor. These GPX genes are upregulated in response to singlet oxygen generator treatment and UV-B irradiation [110]. Unlike non-selenium GPXs from Chlorophyta, non-selenium GPX isolated from E. gracilis uses GSH as an electron donor [111]. In addition to GSH-dependent GPX, the transcriptome data of E. gracilis indicated the existence of three putative Trxdependent GPXs [112]. suggested that microalgae acclimate to environmental stresses by altering cellular glutathione levels. However, to our knowledge, the glutathione synthetic genes in microalgae have not yet been characterized, and thus, the physiological significance of glutathione synthesis is poorly understood.

Glutathione Peroxidase
Glutathione peroxidase (GPX) is an antioxidant enzyme that reduces H2O2, organic hydroperoxides and lipid peroxides, and detoxifies them using GSH or thioredoxin (Trx) as electron donors. During the GPX reaction, GSSG and oxidized Trx are reduced by GR and NADPH-dependent Trx reductase (NTR) ( Figure 5A). GPX is classified into two types: enzyme-containing selenocysteine (SeCys) at the catalytic site and enzyme without SeCys [104,105]. C. reinhardtii contains five genes encoding GPXs, including both SeCyscontaining (GPX1 and GPX2) and non-selenium GPXs (GPX3, GPX4, and GPX5). These GPX enzymes are predicted to be distributed in cellular compartments, including the cytosol, chloroplasts, and mitochondria [106,107]. To date, their functional characterization has been focused on C. reinhardtii GPX5, which uses Trx as an electron donor, and its gene expression is responsive to high light and singlet oxygen generators [108]. Knockout of GPX5 in C. reinhardtii causes ROS accumulation and thereby arrests growth, suggesting the crucial role of GPX5 as an antioxidant enzyme [109]. However, little is known about the physiological functions of GSH-dependent GPX in C. reinhardtii. Chlorella sp. NJ-18 contains two genes encoding non-selenium GPXs, which use Trx as an electron donor. These GPX genes are upregulated in response to singlet oxygen generator treatment and UV-B irradiation [110]. Unlike non-selenium GPXs from Chlorophyta, non-selenium GPX isolated from E. gracilis uses GSH as an electron donor [111]. In addition to GSH-dependent GPX, the transcriptome data of E. gracilis indicated the existence of three putative Trxdependent GPXs [112].

Ascorbate Regeneration
As described in section 3.1.1. GSH is involved in AsA regeneration by providing an electron donor for DHAR. In addition, GSH itself contributes to the non-enzymatic reduction of DHA to AsA in high pH environments. A recent study using A. thaliana demon- Figure 5. Glutathione peroxidase (GPX) reaction (A) and trypanothione (T(SH) 2 ) system (B). GPX uses glutathione (GSH) or thioredoxin (Trx) as electron donors. T(SH) 2 system is biochemically and physiologically characterized in trypanosomatids, and Euglena gracilis contains a set of genes encoding the components of the T(SH) 2 system. GSSG, oxidized glutathione; GR, glutathione reductase; NTR, NADPH-dependent thioredoxin reductase; TS 2 , oxidized trypanothione; TRYR, trypanothione reductase; TXN, tryparedoxin; red, reduced form; ox, oxidized form.

Ascorbate Regeneration
As described in Section 3.1.1. GSH is involved in AsA regeneration by providing an electron donor for DHAR. In addition, GSH itself contributes to the non-enzymatic reduction of DHA to AsA in high pH environments. A recent study using A. thaliana demonstrated that DHAR activity and GSH content cooperatively act as DHA reductants under high light stress conditions [113]. Non-enzymatic DHA regeneration by GSH is assumed to be functional in microalgae.

Heavy Metal Detoxification
Exposure of microalgae to heavy metal ions, such as cadmium, copper, and zinc, causes ROS production and cytotoxicity. GSH and phytochelatins (PCs), which are GSH polymers found in most microalgae, bind to heavy metal ions and detoxify them [114,115]. The general formula of PCs is represented as (γGlu-Cys) n -Gly (PC n ), and microalgae can synthesize those ranging from PC 2 to PC 6 [116][117][118][119][120]. PC synthesis is catalyzed by phytochelatin synthase (PCS), which binds two molecules of GSH to produce PC 2 or GSH and PC n to PC n+1 ( Figure 4); therefore, cellular levels of GSH and its precursor γEC are the key factors in PC synthesis induction. In addition, PCS is activated in the presence of heavy metal ions and promotes PC synthesis [121]. It has been reported that a wide range of microalgae (Chlorophyta C. reinhardtii and D. tertiolecta, Rhodophyta C. merolae, diatoms P. tricornutum and Thalassiosira weissflogii, and Euglenophyta E. gracilis) markedly induced γEC, GSH, and PC synthesis and resisted heavy metal toxicity when exposed to cadmium [116][117][118][119][120][122][123][124][125]. Moreover, the heterologous expression of PCS genes from C. merolae and E. gracilis in yeast confers Cd 2+ tolerance [118,126]. These findings explain the physiological importance of GSH and PC accumulation in microalgae for heavy metal detoxification.
In trypanosomatids, the T(SH) 2 system, which consists of T(SH) 2 , trypanothione reductase (TRYR), and Trx family protein tryparedoxin (TXN), activates target proteins via a dithiol/disulfide exchange reaction ( Figure 5B) [128]. Target proteins of the trypanothione system include peroxiredoxin, which is a thiol peroxidase involved in oxidative stress defense. In addition, T(SH) 2 is able to reduce DHA, thus contributing to APX-dependent ROS scavenging [129]. It has been demonstrated that the T(SH) 2 system plays a crucial role in the survival of parasites exposed to oxidative stress in the host [130,131]. In E. gracilis, the TRYR enzyme was purified from algal cells and biochemically characterized [132]. Genes encoding putative TRYR and TXN were identified in the E. gracilis transcriptome data [112]. Moreover, knockdown of TRYR genes in E. gracilis inhibited growth, suggesting a functional T(SH) 2 system in this algal species [133].

Glutathione-Mediated Redox Regulations
GSH is also known to be involved in redox regulation of photosynthesis and the cell cycle. A previous study using C. reinhardtii identified 10 Calvin cycle enzymes that underwent protein S-glutathionylation, which is a post-translational modification in which GSH is added to the Cys residue of protein under oxidative stress conditions. Among them, the activities of phosphoribulokinase (PRK) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) were demonstrated to be modified by S-glutathionylation [134].
Cell cycle progression is regulated by nuclear GSH. It has been reported that the cell cycle was arrested at the G 1 checkpoint in tobacco cell suspension cultures depleted of GSH levels [100,135]. However, these GSH-mediated redox regulations in microalgae are not fully understood at present, and thus, further investigation is necessary.

Conclusion and Future Perspectives
In all organisms, antioxidant biosynthesis and functions are key factors that determine environmental stress tolerance and cellular process maintenance. Microalgae have evolved antioxidant biosynthesis and function depending on their phylogenetic diversity. As a result, specific carotenoid compounds, such as diadinoxanthin, fucoxanthin, and astaxanthin, as well as the glutathione derivative trypanothione, and many distinct biosynthetic pathways occur in microalgae. This is essential for understanding the cellular metabolism and evolutionary processes of microalgae; however, the findings obtained to date may not be sufficient. Recently, the application of transgenic and genome editing technologies to study microalgae has enabled the modification of their metabolism. Modifications of antioxidant biosynthesis encouraged microalgae researchers to produce high levels of antioxidants and confer resistance to environmental stress. Importantly, as specific carotenoids, such as astaxanthin and fucoxanthin, are known to be effective in maintaining health and preventing disease in humans, carotenoid biosynthesis in microalgae has been actively studied as an attractive target for metabolic modification. In order to understand the evolution and physiology of antioxidants in microalgae and to be able to flexibly design them, future studies should further elucidate their pathways, regulatory mechanisms, and functions.

Data Availability Statement:
The data presented in this study are available in this article.

Conflicts of Interest:
The authors declare no conflict of interest.